首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Chemistry of azoimidazoles: Synthesis, spectral characterization, electrochemical studies, and X-ray crystal structures of isomeric dichloro bis[1-alkyl-2-(arylazo)imidazole] complexes of ruthenium(II)
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Chemistry of azoimidazoles: Synthesis, spectral characterization, electrochemical studies, and X-ray crystal structures of isomeric dichloro bis[1-alkyl-2-(arylazo)imidazole] complexes of ruthenium(II)

机译:偶氮咪唑的化学:钌(II)的异构二氯双[1-烷基-2-(芳基偶氮)咪唑]配合物的合成,光谱表征,电化学研究和X射线晶体结构

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Several new ligands, azoimidazoles belonging to the class 1-methyl-2-(arylazo)imidazoles (L-1 (3)) and 1-benzyl 2-(arylazo)imidazoles (L-2 (4)) (R = H (a), Me (b), OMe (c), Cl (d), NO2 (e)) have been synthesized and reacted with RuCl3 in ethanol under refluxing conditions. Two isomers of the composition RuL2Cl2, green (i) and blue (iii): are chromatographically separated. The green isomer is quantitatively transformed to the blue isomer on refluxing in a high boiling solvent. The isomeric structures have been confirmed by X-ray crystallography. Crystal data are as follows. Green complex C38H34Cl2N8Ru (6a): crystal system monoclinic; space group C2/c; a 15.650(8) Angstrom; b = 22.766(14) Angstrom: c = 11.473(5) Angstrom: beta = 119.27(4)degrees; V = 3573(3) Angstrom(3) Z = 4; R = 3.59%; R-w = 4.38%. Blue complex C22H24Cl2N8Ru(7b): crystal system monoclinic; space group P2(1), a = 9.547(6) Angstrom; b = 22.554(14) Angstrom; c = 11.745(8) Angstrom: beta = 99.07(5)degrees; V = 2498(3) Angstrom(3); Z = 4; R = 3.15%; R-w = 4.51%. With reference to the pairs of Cl, N(imidazole), and N(azo) bound to Ru, the green isomer (6a) has a trans-cis-cis configuration and the blue isomer (7b) is cis-trans-cis. In both structures the Ru-N(azo) distances are relatively shorter than Ru-N(imidazole). indicating stronger bonding in the former and the presence of a Ru-L pi-interaction that is localized in the Ru-azo fragment. The isomer configuration is supported by IR and H-1 NMR data. The compounds exhibit t(2)(Ru) --> pi*(L) MLCT transitions in the visible region. Redox studies show the Ru(TLI)/Ru(II) couple in the green complexes (5, 6) at 0.6-0.7 V and in the blue complexes at 0.7-0.8 V versus SCE and two successive e azo reductions. The difference in the first metal and ligand redox potentials is linearly correlated with nu(CT) (t(2)(Ru) --> pi*(L). [References: 87]
机译:几个新的配体,属于1-甲基-2-(芳基偶氮)咪唑类(L-1(3))和1-苄基2-(芳基偶氮)咪唑类(L-2(4))的偶氮咪唑(R = H( a)合成了Me(b),OMe(c),Cl(d),NO2(e)),并在回流条件下与RuCl3在乙醇中反应。色谱分离了组成为RuL2Cl2的两种异构体:绿色(i)和蓝色(iii):。在高沸点溶剂中回流时,绿色异构体定量转化为蓝色异构体。异构体结构已经通过X射线晶体学证实。晶体数据如下。绿配合物C38H34Cl2N8Ru(6a):晶体系统单斜晶;无定形。空间组C2 / c; 15.650(8)埃; b = 22.766(14)埃:c = 11.473(5)埃:beta = 119.27(4)度; V = 3573(3)埃(3)Z = 4; R = 3.59%; R-w = 4.38%。蓝色络合物C22H24Cl2N8Ru(7b):晶体体系单斜晶;空间群P2(1)/ n,a = 9.547(6)埃; b = 22.554(14)埃; c = 11.745(8)埃:beta = 99.07(5)度; V = 2498(3)埃(3); Z = 4; R = 3.15%; R-w = 4.51%。关于结合至Ru的Cl,N(咪唑)和N(偶氮)对,绿色异构体(6a)具有反式-顺式-顺式构型,蓝色异构体(7b)为顺式-反式-顺式。在两种结构中,Ru-N(偶氮)距离都比Ru-N(咪唑)相对短。表明在前者中有更强的键合,并且存在于Ru-azo片段中的Ru-L pi相互作用存在。 IR和H-1 NMR数据支持异构体构型。这些化合物在可见光区域表现出t(2)(Ru)-> pi *(L)MLCT跃迁。氧化还原研究表明,相对于SCE,Ru(TLI)/ Ru(II)对在绿色配合物(5,6)中的电势为0.6-0.7 V,在蓝色配合物中为0.7-0.8 V的电偶,并且连续发生了两次偶氮还原。第一金属和配体氧化还原电势之差与nu(CT)(t(2)(Ru)-> pi *(L)线性相关。[参考文献:87]

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